Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Microcephaly and DYRK1A[original query] |
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DYRK1A mutations in two unrelated patients. European journal of medical genetics 2015 Mar 58 (3): 168-74. Ruaud Lyse, Mignot Cyril, Guët Agnès, Ohl Christelle, Nava Caroline, Héron Delphine, Keren Boris, Depienne Christel, Benoit Valérie, Maystadt Isabelle, Lederer Damien, Amsallem Daniel, Piard Juliet |
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. Molecular psychiatry 2015 Feb . van Bon B W M, Coe B P, Bernier R, Green C, Gerdts J, Witherspoon K, Kleefstra T, Willemsen M H, Kumar R, Bosco P, Fichera M, Li D, Amaral D, Cristofoli F, Peeters H, Haan E, Romano C, Mefford H C, Scheffer I, Gecz J, de Vries B B A, Eichler E |
DYRK1A-haploinsufficiency in mice causes autistic-like features and febrile seizures. Neurobiology of disease 2017 12 110 180-191. Raveau Matthieu, Shimohata Atsushi, Amano Kenji, Miyamoto Hiroyuki, Yamakawa Kazuhi |
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